Sodium Channel Gene Mutations in Children with GEFS+ and Dravet Syndrome: A Cross Sectional Study

OBJECTIVE: Dravet syndrome or severe myoclonic epilepsy of infancy (SMEI) is a baleful epileptic encephalopathy that begins in the first year of life. This syndrome specified by febrile seizures followed by intractable epilepsy, disturbed psychomotor development, and ataxia. Clinical similarities be...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: TONEKABONI, Seyed Hassan, EBRAHIMI, Ahmad, BAKHSHANDEH BALI, Mohammad Kazem, TAHERI OTAGHSARA, Seyedeh Mohadeseh, HOUSHMAND, Massoud, NASEHI, Mohammad Mahdi, TAGHDIRI, Mohammad Mahdi, MOGHADDASI, Mehdi
Materialtyp: Artigo
Språk:Inglês
Publicerad: Shahid Beheshti University of Medical Sciences 2013
Ämnen:
Original Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3943035/
https://ncbi.nlm.nih.gov/pubmed/24665294
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk